Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/23156
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dc.contributor.authorGhosh, S-
dc.contributor.authorRawat, Preeti-
dc.contributor.authorGupta, S C-
dc.contributor.authorSingh, B P-
dc.date.accessioned2013-11-08T11:32:48Z-
dc.date.available2013-11-08T11:32:48Z-
dc.date.issued2005-06-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/23156-
dc.description536-541en_US
dc.description.abstractA glycoprotein (27 kDa) was isolated from crude somatic antigen of Fasciola gigantica by two steps affinity chromatography and was used in early detection of experimental fasciolosis in cattle by indirect ELISA and in dot-ELISA formats. Although, anti-27 kDa antibodies could be detected after 3 weeks post infection (WPI) by dot - ELISA which was one week later than indirect ELISA. The test, dot-ELISA, was more convenient in field application. By the test (dot-ELISA) the infection could be equally detected in animals infected with 100, 200 and 300 metacercariae of F. gigantica with high sensitivity. Further, the antigen (27 kDa) was not found to react with goat sera infected with Paramphistomum epiclitum, which are giving strong reaction to homologous immature and mature fluke antigens of P. epiclitum.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.43(06) [June 2005]en_US
dc.subjectDot-ELISAen_US
dc.subjectELISAen_US
dc.subjectFaciola giganticen_US
dc.subjectPrepatent diagnosisen_US
dc.titleComparative diagnostic potentiality of ELISA and Dot -ELISA in prepatent diagnosis of experimental Fasciola gigantica infection in cattleen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.43(06) [June 2005]

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